Abstract

The transport of glucose across the cell plasma membrane is vital to most mammalian cells. The glucose transporter (GLUT; also called SLC2A) family of transmembrane solute carriers is responsible for this function in vivo. GLUT proteins encompass 14 different isoforms in humans with different cell type-specific expression patterns and activities. Central to glucose utilization and delivery in the brain is the neuronally expressed GLUT3. Recent research has shown an involvement of GLUT3 genetic variation or altered expression in several different brain disorders, including Huntington’s and Alzheimer’s diseases. Furthermore, GLUT3 was identified as a potential risk gene for multiple psychiatric disorders. To study the role of GLUT3 in brain function and disease a more detailed knowledge of its expression in model organisms is needed. Zebrafish (Danio rerio) has in recent years gained popularity as a model organism for brain research and is now well-established for modeling psychiatric disorders. Here, we have analyzed the sequence of GLUT3 orthologs and identified two paralogous genes in the zebrafish, slc2a3a and slc2a3b. Interestingly, the Glut3b protein sequence contains a unique stretch of amino acids, which may be important for functional regulation. The slc2a3a transcript is detectable in the central nervous system including distinct cellular populations in telencephalon, diencephalon, mesencephalon and rhombencephalon at embryonic and larval stages. Conversely, the slc2a3b transcript shows a rather diffuse expression pattern at different embryonic stages and brain regions. Expression of slc2a3a is maintained in the adult brain and is found in the telencephalon, diencephalon, mesencephalon, cerebellum and medulla oblongata. The slc2a3b transcripts are present in overlapping as well as distinct regions compared to slc2a3a. Double in situ hybridizations were used to demonstrate that slc2a3a is expressed by some GABAergic neurons at embryonic stages. This detailed description of zebrafish slc2a3a and slc2a3b expression at developmental and adult stages paves the way for further investigations of normal GLUT3 function and its role in brain disorders.

Highlights

  • The transport of the monosaccharide glucose across the cell plasma membrane is vital to most mammalian cells and is especially important for brain cells (Cremer, 1964; Norberg and Siesjö, 1974)

  • The phylogenetic analysis suggests that these proteins share a common ancestor and show that both are present in medaka (Oryzias latipes), consistent with a teleost-specific genome duplication (Meyer and Schartl, 1999; Glasauer and Neuhauss, 2014)

  • A comparison of the gene syntenies supports the suggestion that zebrafish slc2a3a and slc2a3b are paralogs and that zebrafish, medaka, mouse and human slc2a3 genes are orthologs (Supplementary Figure S2A)

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Summary

Introduction

The transport of the monosaccharide glucose across the cell plasma membrane is vital to most mammalian cells and is especially important for brain cells (Cremer, 1964; Norberg and Siesjö, 1974). The GLUT family of genes was recently renamed as solute carriers 2A (SLC2A) and includes 14 different isoforms in humans with different cell type-specific expression patterns and functions. This family can be further subdivided into three groups. Type II consists of GLUT5, 7, 9 and 11, and type III includes GLUT6, 8, 10 and 12 (Uldry and Thorens, 2004). Each GLUT protein consists of 12 transmembrane domains, with a central hydrophilic pore as a binding site for glucose, and with both N- and C-termini located in the cytoplasm (Navale and Paranjape, 2016)

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